Q: What do you know about us (Sponsor)? Q: How did you get into Clinical Research? Q: What studies did you work on as a CRC? Q: Have you ever worked with us (Sponsor)? Q: What sponsors did you work with as a CRC? Q: How were you able to bride the gap between being a CRC & a CRA? Q: What phases have you worked on? Q: WHat formal/informal GCP Training have you completed? Q:Are you part of any formalized associations? Q: What did it look lie starting at (CRO)? Did you have a mentor? Q: What made you leave (CRO)? Q: Describe a time you had an issue with a protocol or regulatory compliance & how you handled it? Q: How do you cultivate relationships with the site? Q: What are some bigger sites you've worked at? Q: How do you stay organized? Q: What are your requirements for trip reports? Q: What systems are you currently using? Q: Are you familiar with risk based monitoring?
